Canonical Allele Identifier: CA386881160

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116420268C>G (hg19) ; chr12:g.115982463C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115982463C>G , CM000674.2:g.115982463C>G	GRCh38
NC_000012.11:g.116420268C>G , CM000674.1:g.116420268C>G	GRCh37
NC_000012.10:g.114904651C>G	NCBI36
NG_023366.1:g.299724G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.5096G>C MANE Select	ENSP00000281928.3:p.Trp1699Ser
ENST00000549786.2:c.4524G>C
ENST00000648379.1:n.3464G>C
ENST00000648737.1:n.4860G>C
ENST00000648825.1:n.1836G>C
ENST00000648916.1:n.3107G>C
ENST00000649146.1:n.2339G>C
ENST00000649607.1:c.3280G>C
ENST00000649775.1:c.1585G>C
ENST00000650226.1:c.5096G>C	ENSP00000496981.1:p.Trp1699Ser
ENST00000281928.7:c.5096G>C	ENSP00000281928.3:p.Trp1699Ser
ENST00000549786.1:c.460G>C
ENST00000552340.1:c.128G>C	ENSP00000449876.1:p.Trp43Ser
NM_015335.4:c.5096G>C	NP_056150.1:p.Trp1699Ser
XM_011538080.1:c.5096G>C	XP_011536382.1:p.Trp1699Ser
XM_011538081.1:c.5093G>C	XP_011536383.1:p.Trp1698Ser
XM_011538082.1:c.5066G>C	XP_011536384.1:p.Trp1689Ser
XM_011538080.2:c.5096G>C	XP_011536382.1:p.Trp1699Ser
XM_011538081.2:c.5093G>C	XP_011536383.1:p.Trp1698Ser
XM_011538082.2:c.5066G>C	XP_011536384.1:p.Trp1689Ser
XM_017019090.1:c.5093G>C	XP_016874579.1:p.Trp1698Ser
NM_015335.5:c.5096G>C MANE Select	NP_056150.1:p.Trp1699Ser